Open Access
Volume 21, 2014
Article Number 11
Number of page(s) 10
Published online 10 March 2014

© K.M. Bonney, published by EDP Sciences, 2014

Licence Creative CommonsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Chagas disease (Human American Trypanosomiasis) was first described in 1909 when Carlos Chagas identified the protozoan parasite Trypanosoma cruzi as the cause of an acute febrile illness afflicting Brazilian railroad workers [84]. It is likely that the insect vectors that spread T. cruzi had been transmitting the parasite among wild animals in Central and South America for millions of years before the disease crossed over into domestic animals and humans more than 9000 years ago [7, 26]. Approximately 200–300 years ago, as rapid conversion of the natural forest habitat of the vector into farmland created myriad opportunities for T. cruzi to spread to domesticated animals, Chagas disease became an endemic zoonosis [28]. Urbanization of rural populations in the mid-twentieth century, which involved the migration of large numbers of infected individuals to areas with a comparatively low risk of vectorial transmission, extended the endemic to cities. However, the disease has remained largely confined to poor rural areas. By the end of the twentieth century, Chagas disease had become widely recognized by the World Health Organization (WHO) and other public health authorities as a neglected tropical disease because it primarily affects low-income populations, is a major cause of chronic morbidity and mortality in developing tropical countries, and has been historically underrepresented in the allocation of health-promoting resources from research, governmental, and public aid organizations. Chagas disease is a serious public health burden in Latin America (Table 1), costing the region an estimated 662,000 disability-adjusted life-years (DALYs) of productivity as of 2008, nearly six times the socioeconomic toll of malaria (in terms of DALYs) in the region [48]. Because it disproportionately affects low-income individuals, who are least able to protect themselves against infection and seek and complete appropriate treatment, and has a substantially deleterious effect on the ability of those individuals to pursue education, earn income and save their earnings, Chagas disease is part of a self-propagating cycle of poverty in many endemic regions. More recently, widespread emigration of Latin Americans, including a large number who are infected with T. cruzi, has resulted in an emerging public health threat in historically non-endemic areas of the world such as the United States, Canada, Western Europe, Japan, and Australia (Table 1) [28, 36, 71]. The total economic toll attributed to the disease each year is estimated at over $7 billion USD, with more than 10% of this cost being incurred in the United States and Canada [36, 54].

Table 1.

Estimated number of cases of Trypanosoma cruzi infection by country, as of 2009 [54, 55].

In Latin America, T. cruzi infection most often occurs via vectorial transmission by a type of reduviid bug called a triatomine or “kissing bug”. Triatomines are nocturnal feeders that may live in a variety of environments surrounding human dwellings, including cracks and holes in the walls, ceilings, and floors of substandard housing structures. After taking a blood meal, infected triatomines often excrete feces contaminated with T. cruzi onto their host; T. cruzi can enter the bite wound or a nearby mucosal surface such as the conjunctiva when the victim inadvertently rubs these parasites across their skin [40]. Other routes of transmission include congenital, transfusion of contaminated blood, transplantation of organs from infected donors, ingestion of contaminated food or drinks, and accidental exposure (e.g. laboratory accidents). Once in the bloodstream of a mammalian host, T. cruzi is able to infect a variety of cell types throughout the body and establish a chronic infection.

During the acute phase of T. cruzi infection parasitemia is often high enough that diagnosis can be made through the microscopic examination of blood for the blood-form (trypomastigote stage) of the parasite. During the chronic stage of Chagas disease, diagnosis can be made serologically using enzyme-linked immunosorbent assay, indirect hemagglutination, indirect immunofluorescence, or immunochromatography to test for the presence of T. cruzi-specific immunoglobulin G (IgG). It is recommended that at least two different types of serological tests are used to analyze each potentially infected individual or sample, as notable heterogeneity has been observed among the results obtained using different testing methods, and because there is considerable risk of obtaining false positive results with individual tests due to cross-reactivity of anti-T. cruzi antibodies with antigens of closely related species of trypanosomatids [19, 41, 70, 81]. Thoroughly purifying antigenic preparations prior to analysis and selecting tests with the greatest specificity available can reduce the risk of obtaining false positive results with serological tests. Another potential diagnostic tool for T. cruzi infection is polymerase chain reaction (PCR) to assess the presence of T. cruzi DNA. However, despite promising results for effective use of PCR in the diagnosis of T. cruzi in certain instances in which serological diagnosis may be especially limited, such as in neonates with low parasitemia and in HIV co-infected patients, a combination of serological methods remains the preferred method of diagnosis due to generally higher sensitivity and commercial availability, and lower heterogeneity [19, 31, 41, 70].

After an incubation period of 5–40 days, 10–30% of infected individuals will begin to exhibit non-specific symptoms of acute Chagas disease, including abdominal pain, anorexia, fever, lymphadenopathy, malaise, rash and localized swelling around the site of infection [63]. The mortality rate of acute Chagas disease is 5–10%, usually due to acute myocarditis or meningoencephalitis, with the majority of deaths occurring in young children [82]. However, the majority of T. cruzi-infected individuals become asymptomatic carriers of the parasite, often with low or undetectable parasitemia (though T. cruzi-specific antibodies and DNA may remain at detectable levels in the blood) [1, 77, 83]. After several decades in this indeterminate disease state, during which there are no clinically overt symptoms of organ damage or abnormal electrocardiographic results, approximately 30–40% of asymptomatic carriers will develop chronic Chagas disease characterized by dilated cardiomyopathy leading to congestive heart failure, and/or by development of gastrointestinal disorders, the two most prominent being megacolon and megaesophagus [71]. The etiology of Chagas disease pathogenesis is complex and not completely understood, and may involve a combination of cellular and neuronal damage directly mediated by live T. cruzi, as well as indirect damage caused by immune responses to the parasite and self-antigens exposed during infection [18, 61]. A lengthy period of parasite persistence appears to be necessary for the induction of Chagas pathogenesis [18, 61]. A number of factors, including the host and parasite genetics, infective dose, route of transmission, number of reinfections, and initial and late host immune response affect the onset, severity and presentation of symptoms [5, 8, 20, 27, 38, 63].

Only two drugs, benznidazole and nifurtimox, have been shown to be effective enough to warrant widespread use in Chagas disease treatment. Benznidazole functions, in part, by inducing the formation of free radicals and other metabolites which bind to the nuclear and mitochondrial DNA of T. cruzi, leading to lethal DNA strand breaks [69]. Nifurtimox also exploits the parasite’s vulnerability to oxygen radicals by inhibiting the function of an enzyme T. cruzi requires for detoxifying such compounds [34]. It is widely recommended that treatment with one of these drugs be administered immediately following confirmative diagnosis to those experiencing symptoms of acute Chagas disease. Current treatment protocols are effectively curative in approximately 60% of all acute Chagas cases, but the success rate is only 10–20% for symptomatic chronic Chagas disease, and it remains to be proven whether anti-trypanosomal chemotherapy provides any substantial benefit to patients experiencing the asymptomatic indeterminate state of the disease [4, 12, 15, 23, 74]. Compared with adults, benznidazole treatment of T. cruzi-infected children is considerably more effective and better tolerated [4, 15]. In children, the overall rate of curative therapy has been reported as 71.5% for acute cases of Chagas disease, with >90% cure rates reported for cases of congenital infection if treatment is given within the first year of life [3, 15]. The cure rate of recent chronic Chagas disease in children (0–14 years of age) has been reported as 57.6%; however, this represents a minority of all chronic Chagas patients, as the majority of chronic Chagas patients are 15–69 years of age [3, 42, 58]. It is important to note that anti-T. cruzi treatment efficacy is difficult to accurately assess due to the inherent uncertainty of determining whether and when viable parasites have been completely eliminated from an infected individual. Due to the lack of a reliable early indicator of curative therapy, treatment efficacy is evaluated by the conversion of a previously positive serological test to negative, with long-term follow-up testing for a period of 10–20 years following treatment [52], Consequences of the current inability of physicians to obtain and disseminate timely and accurate information about treatment efficacy to patients include reluctance of patients to complete lengthy treatment regimens and seek follow-up counseling, and impaired ability of physicians to adequately assess and inform patients of their long-term risk of cardiac pathology [52].

In addition to its limited efficacy, treatment with benznidazole or nifurtimox poses a substantial risk of serious side effects, including digestive intolerance, hepatitis, peripheral neuropathy, and rash, which have been observed in 30–50% of treated individuals [36]. Use of these drugs is contraindicated during pregnancy and in patients with advanced kidney or liver disease, and may be logistically or economically prohibitive to other patient populations because a lengthy 60–90 day treatment regimen is often required [36, 71]. Recent estimates place the cost of treatment for an infected individual, depending on the level of care provided, at $46–$7981 USD per year in Colombia and $3000–$14,580 USD per year in Mexico [86]; the per capita GDP in both of these countries is under $10,000 USD according to the International Monetary Fund. These drugs are also not widely available in all areas, and many infected individuals in endemic countries have limited access to health care facilities. Even in the United States these drugs are available only if obtained directly from the Centers for Disease Control (CDC) under an investigational protocol because the United States Food and Drug Administration (FDA) has not yet approved them for routine use in the country. For both of these drugs to be effective, treatment for at least 60 days is required, which compounds the burden of these health, economic, and logistical impediments [71].

Progress against Chagas disease in endemic regions

By some estimates, the number of people infected by T. cruzi worldwide has been reduced by 50% or more within the past 25 years, from a peak of 15–30 million in 1990 [32, 33], to a current total of 8–10 million [89]. After reaching a peak in the 1980s, the number of annual deaths from Chagas disease is estimated to have dropped from 45,000 in 1990 to approximately 12,000 in recent years [32, 60]. Although variations and inherent uncertainties in epidemiological methodology may have resulted in certain studies greatly overestimating the actual prevalence of T. cruzi infection, especially in earlier years, it is clear that extensive public health initiatives in endemic countries have been effective at significantly reducing the rate and risk of new infections.

Control of the insect vector that transmits T. cruzi infection has historically been the primary focus of public health programs aimed at reducing the prevalence of Chagas disease. For the first several decades following the identification of T. cruzi as the causative agent of Chagas disease there was no specific treatment available for human infections and common methods for reducing infestation of domestic dwellings such as the use of kerosene, cyanide gas, or flame throwers were crude and potentially destructive [33]. By the 1940s, focus had shifted to the development of insecticides and improvement of housing structures to limit the persistence and spread of the vector. Because domestic animals, especially dogs, can serve as epidemiologically important reservoirs for the parasite, efforts to eradicate the vector were extended to domestic animal dwellings [44, 59]. By the 1990s, the success of vector eradication programs had become evident in a number of localities and nations, largely due to the success of several large-scale multi-national initiatives.

The most notable of these programs are the Southern Cone Initiative (launched in 1991), the Andean Pact Initiative (launched in 1997) and the Central America Initiative (launched in 1997). The main objectives of these programs were to reduce vectorial transmission by eliminating populations of domestic vectors, to increase screening of blood donors in order to prevent transmission via transfusion, and to expand maternal screening to decrease the incidence of congenital transmission and ensure appropriate treatment of potentially infected neonates. In many regards these programs have been resoundingly successful. By 1999, the Pan-American Health Organization (PAHO) had declared that Triatoma infestans, the primary domestic vector of T. cruzi in rural areas of South America, had been effectively eliminated from human dwellings in Brazil, Chile, Uruguay, and large portions of Argentina, Bolivia, and Paraguay [60, 71, 78]. Efforts to eliminate Rhodnius prolixus, widely considered to be the second most important vector for the transmission of Chagas disease, have been similarly effective in Guatemala, Honduras, and El Salvador, and preliminary results indicate progress is being made in additional areas [33]. Eradication of R. prolixus from all of Central America is now considered feasible in the relatively near future [33]. As a result of vector control, the estimated number of T. cruzi-infected individuals dropped substantially in all ten South American countries targeted by the Southern Cone and Andean Pact Initiatives between 1980 and 2005, as well as for most of the countries targeted by the Central America Initiative [71]. The population deemed at risk for contracting Chagas disease also dropped markedly in the countries targeted by these initiatives. For example, the percent of the Chilean population deemed at risk for contracting the infection dropped from 63% to 5% between 1980 and 2005 [71]; Venezuela experienced a decrease in infection risk from 72% to 18% during the same time period [71].

Following widely successful efforts to reduce vectorial transmission of T. cruzi, blood transfusion became the primary cause of infection in many areas [66]. Mandatory screening of blood products began in many Latin American countries in 1988 [30], and by 2005 100% screening coverage had been achieved in 12 of those countries, with two additional countries achieving 99% coverage [60]. In Brazil, the percent of blood donor candidates who have Chagas disease decreased tenfold in the twenty-five years following 1980, from 4% to 0.4% [33]. These efforts have likely resulted in the prevention of millions of new infections. However, it is notable that the lowest rate of blood donor screening reported by a Latin American country in the aforementioned study, 80%, was in Bolivia [60]. This is of particular importance because Bolivia also has the highest rate of T. cruzi infection in the world, as well as the highest rate of seroprevalence among tested donors [6, 60]. Subsequently, at least one study has indicated that Bolivian immigrants in Europe are more than twice as likely as other Latin American immigrants to be infected with T. cruzi [6].

Congenital transmission accounts for over 15,000 [67] cases of T. cruzi infection each year, mostly in endemic regions, justifying its selection as the third main target of the major Latin American anti-Chagas initiatives of the 1990s. Since the late 1990s, a number of Latin American countries, including Argentina, Uruguay, and Paraguay, have implemented policies to routinely screen all pregnant woman and infants serologically for indications of T. cruzi infection. Because the risk of congenital T. cruzi transmission may last for years after a potential mother initially contracts the infection, and due to widespread emigration of infected individuals, congenital transmission is of concern in both endemic and non-endemic areas, and in areas where vector transmission has been interrupted or eliminated. Due to the substantial side effects and unclear teratogenic risks of available trypanocidal medications and a lack of other therapeutic options, there is no reliable method for preventing congenital infection. The most effective strategy for limiting the spread of congenital Chagas disease is widespread dissemination of available treatment to T. cruzi-infected women of child-bearing age coupled with routine serological screening of pregnant mothers and prompt treatment of children born to infected mothers. Despite therapeutic limitations, extant deficiencies in the requisite diagnostic and clinical infrastructure, and low rates of coverage in impoverished rural areas, there is evidence that the rate of congenital transmission and the morbidity and mortality associated with congenital transmission is declining in a number of areas [78, 85].

The significant decrease in new infections, hospitalizations, loss of healthy years of life and fatalities from Chagas disease achieved by the efforts of successful public health campaigns has resulted in a substantial economic benefit to the world, and to Latin America in particular. Although the sum of this economic benefit is difficult to measure precisely, analysis conducted in the year 2000 estimated that the $420 million USD that the Brazilian government had invested in Chagas disease control between 1975 and 1995 had already resulted in over $3 billion USD in benefits, yielding a net return of $7.16 USD for every dollar invested [2, 33].

The emerging threat of Chagas disease

While the prevalence of Chagas disease in Latin America has been reduced in recent decades, the United States and a number of non-endemic countries in Europe and the Western Pacific Region have experienced a considerable increase in the number of T. cruzi-infected individuals. By the 1980s there had still been no official estimate of the number of T. cruzi-infected individuals in the United States disseminated by the CDC or WHO, and only a small number of cases had been reported in Europe. Currently, the best estimates available place the number of T. cruzi-infected individuals in the United States at over 300,000 [14, 28], with an additional 80,000 residing in Europe [51, 88], and over 10,000 in other non-endemic countries, most notably Australia, Canada, and Japan [71, 89]. These numbers may even be understating the extent of the Chagas disease burden in countries outside of Latin America which lack universal screening systems and whose physicians are often poorly trained in recognizing the disease. Also, the majority of infected individuals in non-endemic countries are Latin American immigrants who often have disproportionately poor access to health care, and are difficult to accurately track and assess from an epidemiological standpoint.

By any estimate, Chagas disease remains a major public health burden today. To illustrate its seriousness, Chagas disease has been labeled “The New HIV/AIDS of the Americas” by prominent scientists due to a number of similarities in epidemiology and societal impact between the two diseases [49]. Chagas disease and AIDS are both chronic conditions caused by blood-borne pathogens that require expensive long-term treatment, and for which there is no effective cure or preventive vaccine. Both diseases affect large numbers of people and exact a substantial social and economic toll. Currently, the number of people infected with T. cruzi in Central and South America is estimated to be over five times the number of people infected with HIV in the same region; however, the global number of HIV infections is higher than the number of T. cruzi-infected individuals [71]. Both diseases pose infection risks to recipients of blood transfusion and organ donation and to children of untreated infected mothers. Moreover, both diseases are highly stigmatized and disproportionately affect individuals living in poverty and least able to access the medical and social support necessary for maintaining the highest possible quality of life. These striking comparisons may prove to be effective at increasing awareness of the seriousness of Chagas disease; however, substantial differences between the infectivity, mortality rate and treatment of the two diseases impose considerable limitations on their comparison. Whereas AIDS is almost always fatal and control of HIV infection requires lifelong antiretroviral treatment, only 20–30% of people infected with Chagas disease will develop potentially fatal cardiomyopathy in their lifetime, and T. cruzi infection is relatively controllable with short-term treatment compared with HIV.

One of the most noteworthy recent developments in broadening understanding of Chagas disease regards not what occurs during T. cruzi infection, but rather where T. cruzi infection occurs. In addition to acknowledging the rapidly increasing number of T. cruzi-infected individuals currently residing in non-endemic countries, it is important to note that not all cases of T. cruzi infection that occur outside of Latin America involve Latin American immigrants who were infected in their countries of origin. One cause of newly acquired T. cruzi infections in countries such as the United States, Spain, Switzerland, and, most recently, Japan is congenital transmission [24, 50, 51, 73]. Although the precise number of congenital Chagas cases in non-endemic countries is unknown [21], it is estimated that 40,000 pregnant women and 2000 newborns are infected with T. cruzi in North America (Canada, Mexico, and the United States) alone. Because T. cruzi-infected neonates are often asymptomatic or exhibit non-specific clinical signs, and obstetrician-gynecologists in non-endemic countries often have limited awareness of Chagas disease and may be less likely to provide the prompt diagnosis and treatment that is crucial for preventing disease progression, congenital transmission is a serious concern that warrants increased attention [24]. Adoption of potentially infected children from endemic regions as well as travel to endemic regions by foreigners may also result in a number of cases of T. cruzi infection in non-endemic countries [28].

There are several additional ways that individuals living outside of Latin America may acquire T. cruzi infection without having lived in or being born to a mother from an endemic region: receipt of contaminated blood products or organs, vectorial transmission, and laboratory accidents. Of these, transmission through blood transfusion or organ transplantation has resulted in the highest number of T. cruzi infections in non-endemic countries, with approximately 20 infections having been recorded in Canada, Spain, and the United States; most or all of these involving donors originating from endemic countries [11, 13, 88]. The United States and France did not begin screening blood donors for the presence of T. cruzi until 2007, and many non-endemic countries either did not start screening for the parasite until even more recently, or still do not engage in widespread screening. As of 2014, Japan still has not implemented routine laboratory-based screening of donated blood for the presence of T. cruzi, and the country also does not customarily screen pregnant mothers for T. cruzi infection, relying instead on a questionnaire to determine whether self-reported risk factors warrant individualized testing [50]. As of January 2014, at least 1900 seropositive donors have been reported in the United States since testing began in 2007, according to the American Association of Blood Banks website. The proportion of US blood donors testing positive for T. cruzi is highest in areas with large numbers of Latin American immigrants, such as Los Angeles and Miami, where the seropositive rates have been reported as 1 in 7500 and 1 in 9000, respectively [56].

As of 2011, only 7% of the 58 organ procurement organizations active in the United States routinely screened all organ donors serologically for T. cruzi, with an additional 12% employing selective screening of high-risk donors [79]. In 2008, 17 donor organs being considered for transplantation into recipients were discarded following a positive test for T. cruzi [79]. Because T. cruzi-infected individuals may remain asymptomatic for decades before developing life-threatening health problems, it is conceivable that additional people have already been infected with the parasite following the receipt of a blood or organ donation and are unaware of their infection status.

Of the 65 cases of T. cruzi infection known to have been acquired via laboratory accidents, at least 11 occurred in the United States or Europe [46]. Although not a similar threat outside of North America, at least seven cases of vectorial transmission of T. cruzi have been verified in the United States since 1955 [13, 22, 35, 47, 65, 76, 90]. The range of triatomine bugs capable of transmitting T. cruzi extends across twenty-six states in the southern half of the country, though infestation of domestic dwellings by triatomine bugs is rare and usually only occurs under atypical conditions, such as following severe droughts [10, 13, 72, 75].

Oral transmission of T. cruzi, which usually occurs due to ingestion of fresh sugar cane or açaí berry juice made from plants harboring infected triatomine bugs, is now the primary cause of T. cruzi infection in some areas of Latin America, such as the Amazonian region of Brazil [80]. Oral transmission has resulted in over 1000 cases of acute Chagas disease in Latin America since the year 2000 [80]. This mode of transmission is considered an emerging threat because outbreaks are sporadic, difficult to predict, and have shown no signs of declining in frequency or severity. The main threat that this route poses to individuals in non-endemic countries is the risk to tourists traveling to areas where consumption of contaminated beverages or foods is most likely.

The future of Chagas disease

Development of an effective vaccine or other new and improved therapies is a crucial, and perhaps the most anticipated and important next step in the fight against Chagas disease [53, 55, 68]. A number of groups are currently in the advanced stages of developing novel therapies, including both DNA- and antigen-based vaccines [36, 37, 43, 62, 68, 87, 91] as well as other anti-trypanosomal drugs including chemical agents that competitively inhibit the function of critical T. cruzi enzymes [16]. Preliminary data demonstrating the efficacy of several of these candidate drugs has been promising, and progress into clinical trials for at least one candidate vaccine which targets two T. cruzi antigens (Tc24 and TSA-1) and includes a TLR4 agonist is likely to occur within the next five years [37]. Benefits of a potential vaccine for T. cruzi compared with the use of standard chemotherapeutic agents include reduced toxicity, allowing for expanded use in chronic patients and patients with comorbidities, potential use during pregnancy to prevent congenital transmission, increased protection against cardiac complications, and removal of treatment barriers associated with the effort and cost of administering repeated drug treatments. Due to the controversial proposition that T. cruzi-induced autoimmunity may play a role in the cardiac pathogenesis of human Chagas disease, it is recommended, even by experts who agree that protective anti-T. cruzi immunity can be promoted by vaccines without the risk of eliciting pathogenic autoimmunity, that vaccine candidates continue to be monitored and tested for this potential risk [36]. In the absence of a rapidly effective cure, work must continue on the development of improved treatments and prognostic indicators for sustained organ damage in chronic Chagas patients, including expanding insight into genetic factors that may influence susceptibility to disease progression and reparative stem cell therapies to ameliorate cardiac damage [8, 29, 38].

Continued progress toward limiting the spread of Chagas disease also requires sustained efforts at widespread vector control [60], refinement of infection and disease risk assessment [38, 64], improvement in the quality of diagnostic tests for screening individuals and the blood supply [1], increased availability of existing therapies and diagnostic tests [57], and expansion of surveillance programs in endemic regions [27, 60]. The Amazonian region of Brazil is of particular importance for surveillance efforts due to the high rate of habitat conversion of previously uninhabited wilderness into dwellings and farmland, creating potential points of contact between T. cruzi and humans [27, 60]. Also, oral transmission of T. cruzi is more prevalent here than anywhere else in the world, and will likely continue to cause a significant number of new infections for many years to come [78, 80]. In addition to maintaining and expanding the aforementioned efforts, endemic countries must continue providing care for the approximately 10 million people already infected with T. cruzi, which will include hospitalizations and other long-term and expensive treatments for many thousands of individuals.

Another important concern in the ongoing effort to control Chagas disease is maintaining a high enough level of political priority to promote and fund surveillance and research at the levels necessary to prevent lapses or regression in the success of public health programs [27, 45, 60]. As stated by Dias et al. [33], “the greatest risk to the current successful trend in Chagas disease control comes, in a sense, from the success that has been achieved.” To elaborate, knowledge of the widespread reduction in the prevalence and risk of T. cruzi infection that has already been achieved may, over time, result in a loss of interest in and commitment to providing and improving surveillance and research and treatment strategies, or a large-scale shifting of resources to more emergent issues. Development of complacency or a lackadaisical attitude toward Chagas disease would carry the risk of allowing a progressive reestablishment of T. cruzi transmission and losing the ability to effectively deal with future outbreaks. Therefore, it is important to maintain robust, centralized public health programs to track and treat T. cruzi transmission, as well as continue to educate the public about the risks of and preventive strategies for the disease.

Additionally, efforts to control the spread of Chagas disease must include increased emphasis on monitoring and controlling globalization of the disease, including the emerging threat of Chagas disease in Europe, Japan, Australia, and the United States and the need for increased surveillance in those areas [6, 9, 13, 27, 28, 39, 49, 60]. Unlike in most regions of Latin America, the number of T. cruzi-infected individuals is rising considerably in non-endemic countries such as the United States, and over 10% of the global healthcare burden related to Chagas disease already originates outside Latin America [54]. Also unlike endemic countries, health care professionals and the public in historically non-endemic countries lack a long history of training and awareness in how to prevent, detect, and treat the disease. In areas where Chagas disease is newly emerging as a major public health concern, as in endemic countries, a crucial part of any successful campaign to limit the spread of T. cruzi infection is education. It is recommended that training in practical methods for identifying and protecting against the vector and for recognizing and seeking treatment for symptoms of potential infection be widely disseminated to primary school educators and community health advocates, in addition to physicians and other health care providers [25]. Increasing awareness of Chagas disease among children is also important since many infections occur during childhood, and because it is the youngest generation that will become the future researchers, health care providers and public policy-makers tasked with the challenge of breaking the self-propagating cycle of a disease that disproportionately affects the poor and further contributes to poverty due to loss of productivity and healthcare costs [17, 25, 78].


There is a growing consensus that Chagas disease, no longer confined to poor rural areas of Latin America, is now a worldwide public health concern and will remain so for the foreseeable future. However, after decades of improvements in surveillance, treatment, and vector-eradication strategies, effective elimination of the disease in the near future is becoming an increasingly attainable goal. Future success in the fight against Chagas disease is dependent upon effective management of newly emerging infectious foci, maintenance of high levels of public awareness and government interest in controlling the disease, and continued improvements in diagnostic, therapeutic, and surveillance tools. Lessons learned from the past 100 years of combating T. cruzi infection must continually be applied and improved upon in order for the next 100 years to yield continued progress against and possibly even eradication of Chagas disease.

Conflict of interest

The author declares no conflicts of interest.


  1. Afonso AM, Ebell MH, Tarleton RL. 2012. A systematic review of high quality diagnostic tests for Chagas disease. PLoS Neglected Tropical Disease, 6(11), e1881. [Google Scholar]
  2. Akhavan D. 2000. Análise de Custo-efetividade do Programa de Controle da Doença de Chagas no Brasil. Organização Pan-Americana da Saúde: Brasília. [Google Scholar]
  3. Altcheh J, Biancardi M, Lapena A, Ballering G, Freilij H. 2005. Congenital Chagas disease: experience in the Hospital de Ninos, Ricardo Gutierrez, Buenos Aires, Argentina. Revista da Sociedade Brasileira de Medicina Tropical, 38(Suppl. 2), 41–45. [PubMed] [Google Scholar]
  4. Altcheh J, Moscatelli G, Moroni S, Garcia-Bournissen F, Freilij H. 2011. Adverse events after the use of benznidazole in infants and children with Chagas disease. Pediatrics, 127(1), e212–e218. [CrossRef] [PubMed] [Google Scholar]
  5. Andrade LO, Machado CR, Chiari E, Pena SD, Macedo AM. 2002. Trypanosoma cruzi: role of host genetic background in the differential tissue distribution of parasite clonal populations. Experimental Parasitology, 100(4), 269–275. [CrossRef] [PubMed] [Google Scholar]
  6. Angheben A, Anselmi M, Gobbi F, Marocco S, Monteiro G, Buonfrate D, Tais S, Talamo M, Zavarise G, Strohmeyer M, Bartalesi F, Mantella A, Di Tommaso M, Aiello K, Veneruso G, Graziani G, Ferrari M, Spreafico I, Bonifacio E, Gaiera G, Lanzafame M, Mascarello M, Cancrini G, Albajar-Vinas P, Bisoffi Z, Bartoloni A. 2011. Chagas disease in Italy: breaking an epidemiological silence. Eurosurveillance, 16(37), 2–9. [Google Scholar]
  7. Aufderheide AC, Salo W, Madden M, Streitz J, Buikstra J, Guhl F, Arriaza B, Renier C, Wittmers LE Jr, Fornaciari G, Allison M. 2004. A 9,000-year record of Chagas’ disease. Proceedings of the National Academy of Sciences of the United States of America, 101(7), 2034–2039. [CrossRef] [PubMed] [Google Scholar]
  8. Ayo CM, Dalalio MM, Visentainer JE, Reis PG, Sippert EA, Jarduli LR, Alves HV, Sell AM. 2013. Genetic susceptibility to Chagas disease: an overview about the infection and about the association between disease and the immune response genes. Biomed Research International, 2013, 284729. [Google Scholar]
  9. Basile L, Jansa JM, Carlier Y, Salamanca DD, Angheben A, Bartoloni A, Seixas J, Van Gool T, Canavate C, Flores-Chavez M, Jackson Y, Chiodini PL, Albajar-Vinas P. 2011. Chagas disease in European countries: the challenge of a surveillance system. Eurosurveillance, 16(37), 14–23. [Google Scholar]
  10. Beard CB, Pye G, Steurer FJ, Rodriguez R, Campman R, Peterson AT, Ramsey J, Wirtz RA, Robinson LE. 2003. Chagas disease in a domestic transmission cycle, southern Texas, USA. Emerging Infectious Diseases, 9(1), 103–105. [CrossRef] [PubMed] [Google Scholar]
  11. Benjamin RJ, Stramer SL, Leiby DA, Dodd RY, Fearon M, Castro E. 2012. Trypanosoma cruzi infection in North America and Spain: evidence in support of transfusion transmission. Transfusion, 52(9), 1913–1921, quiz 1912. [CrossRef] [PubMed] [Google Scholar]
  12. Bern C. 2011. Antitrypanosomal therapy for chronic Chagas’ disease. New England Journal of Medicine, 364(26), 2527–2534. [CrossRef] [Google Scholar]
  13. Bern C, Kjos S, Yabsley MJ, Montgomery SP. 2011. Trypanosoma cruzi and Chagas’ disease in the United States. Clinical Microbiology Reviews, 24(4), 655–681. [CrossRef] [PubMed] [Google Scholar]
  14. Bern C, Montgomery SP. 2009. An estimate of the burden of Chagas disease in the United States. Clinical Infectious Diseases, 49(5), e52–e54. [CrossRef] [Google Scholar]
  15. Bern C, Montgomery SP, Herwaldt BL, Rassi A Jr, Marin-Neto JA, Dantas RO, Maguire JH, Acquatella H, Morillo C, Kirchhoff LV, Gilman RH, Reyes PA, Salvatella R, Moore AC. 2007. Evaluation and treatment of chagas disease in the United States: a systematic review. Journal of the American Medical Association, 298(18), 2171–2181. [CrossRef] [PubMed] [Google Scholar]
  16. Berneman A, Montout L, Goyard S, Chamond N, Cosson A, d’Archivio S, Gouault N, Uriac P, Blondel A, Minoprio P. 2013. Combined approaches for drug design points the way to novel proline racemase inhibitor candidates to fight Chagas’ disease. PLoS One, 8(4), e60955. [CrossRef] [PubMed] [Google Scholar]
  17. Bonney KM. 2013. An argument and plan for promoting the teaching and learning of neglected tropical diseases. Journal of Microbiology and Biology Education, 14(2), 183–188. [CrossRef] [Google Scholar]
  18. Bonney KM, Engman DM. 2008. Chagas heart disease pathogenesis: one mechanism or many? Current Molecular Medicine, 8(6), 510–518. [CrossRef] [PubMed] [Google Scholar]
  19. Brasil PE, De Castro L, Hasslocher-Moreno AM, Sangenis LH, Braga JU. 2010. ELISA versus PCR for diagnosis of chronic Chagas disease: systematic review and meta-analysis. BMC Infectious Disease, 10, 337. [CrossRef] [Google Scholar]
  20. Brener Z, Gazzinelli RT. 1997. Immunological control of Trypanosoma cruzi infection and pathogenesis of Chagas’ disease. International Archives of Allergy and Immunology, 114(2), 103–110. [CrossRef] [PubMed] [Google Scholar]
  21. Buekens P, Almendares O, Carlier Y, Dumonteil E, Eberhard M, Gamboa-Leon R, James M, Padilla N, Wesson D, Xiong X. 2008. Mother-to-child transmission of Chagas’ disease in North America: why don’t we do more? Maternal and Child Health Journal, 12(3), 283–286. [CrossRef] [PubMed] [Google Scholar]
  22. Cantey PT, Stramer SL, Townsend RL, Kamel H, Ofafa K, Todd CW, Currier M, Hand S, Varnado W, Dotson E, Hall C, Jett PL, Montgomery SP. 2012. The United States Trypanosoma cruzi Infection Study: evidence for vector-borne transmission of the parasite that causes Chagas disease among United States blood donors. Transfusion, 52(9), 1922–1930. [CrossRef] [PubMed] [Google Scholar]
  23. Carlier Y, Torrico F, Sosa-Estani S, Russomando G, Luquetti A, Freilij H, Albajar Vinas P. 2011. Congenital Chagas disease: recommendations for diagnosis, treatment and control of newborns, siblings and pregnant women. PLoS Neglected Tropical Disease, 5(10), e1250. [CrossRef] [Google Scholar]
  24. CDC. 2010. Congenital Transmission of Chagas Disease – Virginis, 2010. Morbidity and Mortality Weekly Report (MMWR) (July 6, 2012, 61(26), 477–479). [Google Scholar]
  25. Coura JR. 2007. Chagas disease: what is known and what is needed – a background article. Memórias do Instituto Oswaldo Cruz, 102(Suppl 1), 113–122. [Google Scholar]
  26. Coura JR, Borges-Pereira J. 2010. Chagas disease: 100 years after its discovery. A systemic review. Acta Tropica, 115(1–2), 5–13. [CrossRef] [PubMed] [Google Scholar]
  27. Coura JR, Borges-Pereira J. 2012. Chagas disease. What is known and what should be improved: a systemic review. Revista da Sociedade Brasileira de Medicina Tropical, 45(3), 286–296. [CrossRef] [PubMed] [Google Scholar]
  28. Coura JR, Vinas PA. 2010. Chagas disease: a new worldwide challenge. Nature, 465(7301), S6–S7. [CrossRef] [PubMed] [Google Scholar]
  29. de Carvalho KA, Abdelwahid E, Ferreira RJ, Irioda AC, Guarita-Souza LC. 2013. Preclinical stem cell therapy in Chagas Disease: Perspectives for future research. World Journal of Transplant, 3(4), 119–126. [Google Scholar]
  30. De Paula EV, Goncales NS, Xueref S, Addas-Carvalho M, Gilli SC, Angerami RN, Goncales FL Jr. 2008. Prevalence of transfusion-transmitted Chagas Disease among multitransfused patients in Brazil. BMC Infectious Disease, 8, 5. [CrossRef] [Google Scholar]
  31. De Winne K, Buscher P, Luquetti AO, Tavares SB, Oliveira RA, Solari A, Zulantay I, Apt W, Diosque P, Monje Rumi M, Girones N, Fresno M, Lopez-Velez R, Perez-Molina JA, Monge-Maillo B, Garcia L, Deborggraeve S. 2014. The Trypanosoma cruzi satellite DNA OligoC-TesT and Trypanosoma cruzi Kinetoplast DNA OligoC-TesT for diagnosis of Chagas disease: A multi-cohort comparative evaluation study. PLoS Neglected Tropical Disease, 8(1), e2633. [CrossRef] [Google Scholar]
  32. Dias JC, Prata A, Correia D. 2008. Problems and perspectives for Chagas disease control: in search of a realistic analysis. Revista da Sociedade Brasileira de Medicina Tropical, 41(2), 193–196. [PubMed] [Google Scholar]
  33. Dias JC, Silveira AC, Schofield CJ. 2002. The impact of Chagas disease control in Latin America: a review. Memórias do Instituto Oswaldo Cruz, 97(5), 603–612. [CrossRef] [Google Scholar]
  34. Docampo R, Moreno SN. 1986. Free radical metabolism of antiparasitic agents. Federation Proceedings, 45(10), 2471–2476. [PubMed] [Google Scholar]
  35. Dorn PL, Perniciaro L, Yabsley MJ, Roellig DM, Balsamo G, Diaz J, Wesson D. 2007. Autochthonous transmission of Trypanosoma cruzi, Louisiana. Emerging Infectious Diseases, 13(4), 605–607. [CrossRef] [PubMed] [Google Scholar]
  36. Dumonteil E, Bottazzi ME, Zhan B, Heffernan MJ, Jones K, Valenzuela JG, Kamhawi S, Ortega J, Rosales SP, Lee BY, Bacon KM, Fleischer B, Slingsby BT, Cravioto MB, Tapia-Conyer R, Hotez PJ. 2012. Accelerating the development of a therapeutic vaccine for human Chagas disease: rationale and prospects. Expert Review of Vaccines, 11(9), 1043–1055. [CrossRef] [PubMed] [Google Scholar]
  37. Dumonteil E, Escobedo-Ortegon J, Reyes-Rodriguez N, Arjona-Torres A, Ramirez-Sierra MJ. 2004. Immunotherapy of Trypanosoma cruzi infection with DNA vaccines in mice. Infection and Immunity, 72(1), 46–53. [CrossRef] [PubMed] [Google Scholar]
  38. Frade AF, Pissetti CW, Ianni BM, Saba B, Lin-Wang HT, Nogueira LG, de Melo Borges A, Buck P, Dias F, Baron M, Ferreira LR, Schmidt A, Marin-Neto JA, Hirata M, Sampaio M, Fragata A, Pereira AC, Donadi E, Kalil J, Rodrigues V, Cunha-Neto E, Chevillard C. 2013. Genetic susceptibility to Chagas disease cardiomyopathy: involvement of several genes of the innate immunity and chemokine-dependent migration pathways. BMC Infectious Disease, 13, 587. [CrossRef] [Google Scholar]
  39. Gascon J, Bern C, Pinazo MJ. 2010. Chagas disease in Spain, the United States and other non-endemic countries. Acta Tropica, 115(1–2), 22–27. [CrossRef] [PubMed] [Google Scholar]
  40. Giddings OK, Eickhoff CS, Smith TJ, Bryant LA, Hoft DF. 2006. Anatomical route of invasion and protective mucosal immunity in Trypanosoma cruzi conjunctival infection. Infection and Immunity, 74(10), 5549–5560. [CrossRef] [PubMed] [Google Scholar]
  41. Gilber SR, Alban SM, Gobor L, Bescrovaine Jde O, Myiazaki MI, Thomaz-Soccol V. 2013. Comparison of conventional serology and PCR methods for the routine diagnosis of Trypanosoma cruzi infection. Revista da Sociedade Brasileira de Medicina Tropical, 46(3), 310–315. [CrossRef] [PubMed] [Google Scholar]
  42. Guedes PM, Silva GK, Gutierrez FR, Silva JS. 2011. Current status of Chagas disease chemotherapy. Expert Review of Anti Infective Therapy, 9(5), 609–620. [CrossRef] [Google Scholar]
  43. Gupta S, Garg NJ. 2013. TcVac3 induced control of Trypanosoma cruzi infection and chronic myocarditis in mice. PLoS One, 8(3), e59434. [CrossRef] [PubMed] [Google Scholar]
  44. Gurtler RE, Cecere MC, Lauricella MA, Cardinal MV, Kitron U, Cohen JE. 2007. Domestic dogs and cats as sources of Trypanosoma cruzi infection in rural northwestern Argentina. Parasitology, 134(Pt 1), 69–82. [CrossRef] [PubMed] [Google Scholar]
  45. Gurtler RE, Diotaiuti L, Kitron U. 2008. Commentary: Chagas disease: 100 years since discovery and lessons for the future. International Journal of Epidemiology, 37(4), 698–701. [CrossRef] [PubMed] [Google Scholar]
  46. Herwaldt BL. 2001. Laboratory-acquired parasitic infections from accidental exposures. Clinical Microbiology Reviews, 14(4), 659–688. [CrossRef] [PubMed] [Google Scholar]
  47. Herwaldt BL, Grijalva MJ, Newsome AL, McGhee CR, Powell MR, Nemec DG, Steurer FJ, Eberhard ML. 2000. Use of polymerase chain reaction to diagnose the fifth reported US case of autochthonous transmission of Trypanosoma cruzi, in Tennessee, 1998. Journal of Infectious Diseases, 181(1), 395–399. [CrossRef] [Google Scholar]
  48. Hotez PJ, Bottazzi ME, Franco-Paredes C, Ault SK, Periago MR. 2008. The neglected tropical diseases of Latin America and the Caribbean: a review of disease burden and distribution and a roadmap for control and elimination. PLoS Neglected Tropical Disease, 2(9), e300. [CrossRef] [Google Scholar]
  49. Hotez PJ, Dumonteil E, Woc-Colburn L, Serpa JA, Bezek S, Edwards MS, Hallmark CJ, Musselwhite LW, Flink BJ, Bottazzi ME. 2012. Chagas disease: “the new HIV/AIDS of the Americas”. PLoS Neglected Tropical Disease, 6(5), e1498. [CrossRef] [Google Scholar]
  50. Imai K, Maeda T, Sayama Y, Mikita K, Fujikura Y, Misawa K, Nagumo M, Iwata O, Ono T, Kurane I, Miyahira Y, Kawana A, Miura S. 2014. Mother-to-child transmission of congenital Chagas disease, Japan. Emerging Infectious Diseases, 20(1), 146–148. [CrossRef] [PubMed] [Google Scholar]
  51. Jackson Y, Chappuis F. 2011. Chagas disease in Switzerland: history and challenges. Eurosurveillance, 16(37), 10–13. [Google Scholar]
  52. Jackson Y, Chatelain E, Mauris A, Holst M, Miao Q, Chappuis F, Ndao M. 2013. Serological and parasitological response in chronic Chagas patients 3 years after nifurtimox treatment. BMC Infectious Disease, 13, 85. [CrossRef] [Google Scholar]
  53. Le Loup G, Pialoux G, Lescure FX. 2011. Update in treatment of Chagas disease. Current Opinion in Infectious Diseases, 24(5), 428–434. [CrossRef] [PubMed] [Google Scholar]
  54. Lee BY, Bacon KM, Bottazzi ME, Hotez PJ. 2013. Global economic burden of Chagas disease: a computational simulation model. Lancet Infectious Diseases, 13(4), 342–348. [CrossRef] [Google Scholar]
  55. Lee BY, Bacon KM, Wateska AR, Bottazzi ME, Dumonteil E, Hotez PJ. 2012. Modeling the economic value of a Chagas’ disease therapeutic vaccine. Human Vaccines and Immunotherapeutics, 8(9), 1293–1301. [CrossRef] [Google Scholar]
  56. Leiby DA, Herron RM Jr, Read EJ, Lenes BA, Stumpf RJ. 2002. Trypanosoma cruzi in Los Angeles and Miami blood donors: impact of evolving donor demographics on seroprevalence and implications for transfusion transmission. Transfusion, 42(5), 549–555. [CrossRef] [PubMed] [Google Scholar]
  57. Manne JM, Snively CS, Ramsey JM, Salgado MO, Barnighausen T, Reich MR. 2013. Barriers to treatment access for Chagas disease in Mexico. PLoS Neglected Tropical Disease, 7(10), e2488. [CrossRef] [Google Scholar]
  58. Matta Guedes PM, Gutierrez FR, Nascimento MS, Do-Valle-Matta MA, Silva JS. 2012. Antiparasitical chemotherapy in Chagas’ disease cardiomyopathy: current evidence. Tropical Medicine and International Health, 17(9), 1057–1065. [CrossRef] [Google Scholar]
  59. Miles MA, Feliciangeli MD, de Arias AR. 2003. American trypanosomiasis (Chagas’ disease) and the role of molecular epidemiology in guiding control strategies. British Medical Journal, 326(7404), 1444–1448. [CrossRef] [PubMed] [Google Scholar]
  60. Moncayo A, Silveira AC. 2009. Current epidemiological trends for Chagas disease in Latin America and future challenges in epidemiology, surveillance and health policy. Memórias do Instituto Oswaldo Cruz, 104(Suppl 1), 17–30. [CrossRef] [Google Scholar]
  61. Nagajyothi F, Machado FS, Burleigh BA, Jelicks LA, Scherer PE, Mukherjee S, Lisanti MP, Weiss LM, Garg NJ, Tanowitz HB. 2012. Mechanisms of Trypanosoma cruzi persistence in Chagas disease. Cellular Microbiology, 14(5), 634–643. [CrossRef] [PubMed] [Google Scholar]
  62. Nakayasu ES, Sobreira TJ, Torres R Jr, Ganiko L, Oliveira PS, Marques AF, Almeida IC. 2012. Improved proteomic approach for the discovery of potential vaccine targets in Trypanosoma cruzi. Journal of Proteome Research, 11(1), 237–246. [CrossRef] [PubMed] [Google Scholar]
  63. Nobrega AA, Garcia MH, Tatto E, Obara MT, Costa E, Sobel J, Araujo WN. 2009. Oral transmission of Chagas disease by consumption of acai palm fruit, Brazil. Emerging Infectious Diseases, 15(4), 653–655. [CrossRef] [PubMed] [Google Scholar]
  64. Nouvellet P, Dumonteil E, Gourbiere S. 2013. The improbable transmission of Trypanosoma cruzi to human: the missing link in the dynamics and control of Chagas disease. PLoS Neglected Tropical Disease, 7(11), e2505. [CrossRef] [Google Scholar]
  65. Ochs DE, Hnilica VS, Moser DR, Smith JH, Kirchhoff LV. 1996. Postmortem diagnosis of autochthonous acute chagasic myocarditis by polymerase chain reaction amplification of a species-specific DNA sequence of Trypanosoma cruzi. American Journal of Tropical Medicine and Hygiene, 54(5), 526–529. [Google Scholar]
  66. Oelemann WM, Teixeira MD, Verissimo Da Costa GC, Borges-Pereira J, De Castro JA, Coura JR, Peralta JM. 1998. Evaluation of three commercial enzyme-linked immunosorbent assays for diagnosis of Chagas’ disease. Journal of Clinical Microbiology, 36(9), 2423–2427. [PubMed] [Google Scholar]
  67. Organization PAH. 2007. Report of the technical consultation on information, education and communication (IEC) on congenital Chagas’ disease, OPS/HDM/CD/476/07. [Google Scholar]
  68. Quijano-Hernandez I, Dumonteil E. 2011. Advances and challenges towards a vaccine against Chagas disease. Human Vaccines, 7(11), 1184–1191. [CrossRef] [PubMed] [Google Scholar]
  69. Rajao MA, Furtado C, Alves CL, Passos-Silva DG, de Moura MB, Schamber-Reis BL, Kunrath-Lima M, Zuma AA, Vieira-da-Rocha JP, Borio Ferreira Garcia J, Mendes IC, Junho Pena SD, Macedo AM, Franco GR, de Souza-Pinto NC, de Medeiros MH, Cruz AK, Machado Motta MC, Ribeiro Teixeira SM, Machado CR. 2013. Unveiling Benznidazole’s mechanism of action through overexpression of DNA repair proteins in Trypanosoma cruzi. Environmental and Molecular Mutagenesis. [Google Scholar]
  70. Ramirez JD, Guhl F, Umezawa ES, Morillo CA, Rosas F, Marin-Neto JA, Restrepo S. 2009. Evaluation of adult chronic Chagas’ heart disease diagnosis by molecular and serological methods. Journal of Clinical Microbiology, 47(12), 3945–3951. [CrossRef] [PubMed] [Google Scholar]
  71. Rassi A Jr, Rassi A, Marin-Neto JA. 2010. Chagas disease. Lancet, 375(9723), 1388–1402. [CrossRef] [PubMed] [Google Scholar]
  72. Reisenman CE, Lawrence G, Guerenstein PG, Gregory T, Dotson E, Hildebrand JG. 2010. Infection of kissing bugs with Trypanosoma cruzi, Tucson, Arizona, USA. Emerging Infectious Diseases, 16(3), 400–405. [CrossRef] [PubMed] [Google Scholar]
  73. Riera C, Guarro A, Kassab HE, Jorba JM, Castro M, Angrill R, Gallego M, Fisa R, Martin C, Lobato A, Portus M. 2006. Congenital transmission of Trypanosoma cruzi in Europe (Spain): a case report. American Journal of Tropical Medicine and Hygiene, 75(6), 1078–1081. [Google Scholar]
  74. Rodriques Coura J, de Castro SL. 2002. A critical review on Chagas disease chemotherapy. Memórias do Instituto Oswaldo Cruz, 97(1), 3–24. [Google Scholar]
  75. Roellig DM, Savage MY, Fujita AW, Barnabe C, Tibayrenc M, Steurer FJ, Yabsley MJ. 2013. Genetic variation and exchange in Trypanosoma cruzi isolates from the United States. PLoS One, 8(2), e56198. [CrossRef] [PubMed] [Google Scholar]
  76. Schiffler RJ, Mansur GP, Navin TR, Limpakarnjanarat K. 1984. Indigenous Chagas’ disease (American trypanosomiasis) in California. Journal of the American Medical Association, 251(22), 2983–2984. [CrossRef] [PubMed] [Google Scholar]
  77. Schijman AG, Bisio M, Orellana L, Sued M, Duffy T, Mejia Jaramillo AM, Cura C, Auter F, Veron V, Qvarnstrom Y, Deborggraeve S, Hijar G, Zulantay I, Lucero RH, Velazquez E, Tellez T, Sanchez Leon Z, Galvao L, Nolder D, Monje Rumi M, Levi JE, Ramirez JD, Zorrilla P, Flores M, Jercic MI, Crisante G, Anez N, De Castro AM, Gonzalez CI, Acosta Viana K, Yachelini P, Torrico F, Robello C, Diosque P, Triana Chavez O, Aznar C, Russomando G, Buscher P, Assal A, Guhl F, Sosa Estani S, DaSilva A, Britto C, Luquetti A, Ladzins J. 2011. International study to evaluate PCR methods for detection of Trypanosoma cruzi DNA in blood samples from Chagas disease patients. PLoS Neglected Tropical Disease, 5(1), e931. [Google Scholar]
  78. Schofield CJ, Jannin J, Salvatella R. 2006. The future of Chagas disease control. Trends in Parasitology, 22(12), 583–588. [CrossRef] [PubMed] [Google Scholar]
  79. Schwartz BS, Paster M, Ison MG, Chin-Hong PV. 2011. Organ donor screening practices for Trypanosoma cruzi infection among US Organ Procurement Organizations. American Journal of Transplantation, 11(4), 848–851. [CrossRef] [Google Scholar]
  80. Shikanai-Yasuda MA, Carvalho NB. 2012. Oral transmission of Chagas disease. Clinical Infectious Diseases, 54(6), 845–852. [CrossRef] [Google Scholar]
  81. Souza RM, Amato Neto V. 2012. Discrepancies and consequences of indirect hemagglutination, indirect immunofluorescence and ELISA tests for the diagnosis of Chagas disease. Revista do Instituto de Medicina Tropical de Sao Paulo, 54(3), 141–143. [CrossRef] [PubMed] [Google Scholar]
  82. Tanowitz HB, Kirchhoff LV, Simon D, Morris SA, Weiss LM, Wittner M. 1992. Chagas’ disease. Clinical Microbiology Reviews, 5, 400–419. [PubMed] [Google Scholar]
  83. Teixeira AR, Nascimento RJ, Sturm NR. 2006. Evolution and pathology in Chagas disease – a review. Memórias do Instituto Oswaldo Cruz, 101(5), 463–491. [CrossRef] [Google Scholar]
  84. Tibayrenc M, Telleria J. 2010. American trypanosomiasis: Chagas disease: one hundred years of research, 1st edn. Elsevier insights. Elsevier: London; Burlington, MA, USA, 848 p. [Google Scholar]
  85. Torrico F, Alonso-Vega C, Suarez E, Rodriguez P, Torrico MC, Dramaix M, Truyens C, Carlier Y. 2004. Maternal Trypanosoma cruzi infection, pregnancy outcome, morbidity, and mortality of congenitally infected and non-infected newborns in Bolivia. American Journal of Tropical Medicine and Hygiene, 70(2), 201–209. [Google Scholar]
  86. Vallejo M, Montenegro P, Reyes PA. 2002. How much does the medical treatment of chronic Chagas cardiopathy cost? Direct costs in a cardiology hospital. Archivos de Cardiologia de Mexico, 72(2), 129–137. [PubMed] [Google Scholar]
  87. Vazquez-Chagoyan JC, Gupta S, Garg NJ. 2011. Vaccine development against Trypanosoma cruzi and Chagas disease. Advances in Parasitology, 75, 121–146. [CrossRef] [PubMed] [Google Scholar]
  88. WHO. 2009. Control and prevention of Chagas disease in Europe. Report of a WHO Informal Consultation (jointly organized by WHO headquarters and the WHO Regional Office for Europe. [Google Scholar]
  89. WHO. 2010. Working to overcome the global impact of neglected tropical diseases. First WHO report on neglected tropical diseases. [Google Scholar]
  90. Woody NC, Woody HB. 1955. American trypanosomiasis (Chagas’ disease); first indigenous case in the United States. Journal of the American Medical Association, 159(7), 676–677. [CrossRef] [PubMed] [Google Scholar]
  91. Zapata-Estrella H, Hummel-Newell C, Sanchez-Burgos G, Escobedo-Ortegon J, Ramirez-Sierra MJ, Arjona-Torres A, Dumonteil E. 2006. Control of Trypanosoma cruzi infection and changes in T-cell populations induced by a therapeutic DNA vaccine in mice. Immunology Letters, 103(2), 186–191. [CrossRef] [PubMed] [Google Scholar]

Cite this article as: Bonney KM: Chagas disease in the 21st Century: a public health success or an emerging threat? Parasite, 2014, 21, 11.

All Tables

Table 1.

Estimated number of cases of Trypanosoma cruzi infection by country, as of 2009 [54, 55].

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